Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:121928459-121928510 | Rare:12 | ||||
chr10:122019181-122019444 | Rare:49 | ||||
chr10:122019502-122019848 | Common:5; Rare:58 | ||||
chr10:122126881-122127069 | Common:1; Rare:41 | ||||
chr10:122879544-122879681 | Common:3; Rare:40 | ||||
chr10:122954197-122954486 | Rare:107 | ||||
chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092412-124092613 | Common:1; Rare:51 | ||||
chr10:124418875-124419092 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
chr10:124791745-124791938 | Common:1; Rare:102 | ||||
chr10:125719462-125719744 | Common:1; Rare:97 | ||||
chr10:125823207-125823615 | Common:1; Rare:145; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896293-125896619 | Common:5; Rare:27 | ||||
chr10:133308835-133309094 | Common:2; Rare:104 | ||||
chr11:207363-207715 | Common:7; Rare:109 |